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dbVar

Database of genomic structural variation

nsv7009177

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:294,850

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1474 SVs from 91 studies. See in: genome view

Submitted genomic22,848,905-23,143,754

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7009177	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	22,848,905	23,143,754
nsv7009177	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	23,031,707	23,326,556

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18421757	deletion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18421757	Submitted genomic		NC_000019.10:g.228 48905_23143754del	GRCh38 (hg38)		NC_000019.10	Chr19	22,848,905	23,143,754
nssv18421757	Remapped	Perfect	NC_000019.9:g.2303 1707_23326556del	GRCh37.p13	First Pass	NC_000019.9	Chr19	23,031,707	23,326,556

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18421757	7e-06	2	275780

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